Evidence map›Paper›PMID 20028761›Full record

ReviewClinical cancer research : an official journal of the American Association for Cancer Research2010

Immunotherapy of malignant disease with tumor antigen-specific monoclonal antibodies.

Michael Campoli, Robert Ferris, Soldano Ferrone, Xinhui Wang

Open access · bronzeAbstract readReview
In one paragraph

Review in Clinical cancer research : an official journal of the American Association for Cancer Research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
8.3field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 70 citations in OpenAlex.

  1. Trial
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  7. Article
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  9. Article
  10. Review
  11. Article
  12. Biological therapy and dentistry: a review paper.Oral surgery, oral medicine, oral pathology and oral radiology · 2015
    Review
  13. Article
  14. New targeted therapies in pancreatic cancer.World journal of gastroenterology · 2015
    Review
  15. Review
  16. Review
  17. Article
  18. IgE immunotherapy against cancer.Current topics in microbiology and immunology · 2015
    Review
  19. Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Michael CampoliDepartment of Dermatology, University of Colorado Health Science Center, Denver, Colorado, USA.
Robert Ferris
Soldano Ferrone
Xinhui Wang
UPMC Hillman Cancer Center · USUniversity of Colorado Health · US

Funding

WILD TYPE P53-BASED ADJUVANT IMMUNOTHERAPY FOR SCCHNP50CA097190 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHRISTOPHER J. BAKKENIST · 2004 to 2026
$49.6M
Immune activation by cetuximab in head and neck cancer patientsR01DE019727 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FERRIS, ROBERT L. · 2010 to 2014
$2.0M
Rational Design of HMW-MAA Peptide MimicsR01CA105500 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FERRONE, SOLDANO · 2004 to 2008
$1.6M
Antigen processing and HLA-peptide complexes in head and neck cancerR01CA110249 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FERRONE, SOLDANO · 2006 to 2010
$1.5M
HLA classl complex expression in breast cancer immunityR01CA113861 · NCI · MAYO CLINIC ROCHESTER · PI KNUTSON, KEITH L. · 2005 to 2009
$1.1M
NCI NIH HHS IPSO CA097190NCI NIH HHS R01CA10494NCI NIH HHS R01 CA105500NCI NIH HHS R01CA105500NCI NIH HHS R01 CA110249NCI NIH HHS R01CA110249NCI NIH HHS R01 CA113861NCI NIH HHS R01CA113861NIDCR NIH HHS R01 DE19727PHS HHS R03 RFA PA-08-209
6 · The paper itself

Abstract

A few tumor antigen (TA)-specific monoclonal antibodies (mAb) have been approved by the Food and Drug Administration for the treatment of several major malignant diseases and are commercially available. Once in the clinic, mAbs have an average success rate of approximately 30% and are well tolerated. These results have changed the face of cancer therapy, bringing us closer to more specific and more effective biological therapy of cancer. The challenge facing tumor immunologists at present is represented by the identification of the mechanism(s) underlying the patients' differential clinical response to mAb-based immunotherapy. This information is expected to lead to the development of criteria to select patients to be treated with mAb-based immunotherapy. In the past, in vitro and in vivo evidence has shown that TA-specific mAbs can mediate their therapeutic effect by inducing tumor cell apoptosis, inhibiting the targeted antigen function, blocking tumor cell signaling, and/or mediating complement- or cell-dependent lysis of tumor cells. More recent evidence suggests that TA-specific mAb can induce TA-specific cytotoxic T-cell responses by enhancing TA uptake by dendritic cells and cross-priming of T cells. In this review, we briefly summarize the TA-specific mAbs that have received Food and Drug Administration approval. Next, we review the potential mechanisms underlying the therapeutic efficacy of TA-specific mAbs with emphasis on the induction of TA-specific cellular immune responses and their potential to contribute to the clinical efficacy of TA-specific mAb-based immunotherapy. Lastly, we discuss the potential negative effect of immune escape mechanisms on the clinical efficacy of TA-specific mAb-based immunotherapy.

Indexed as

Antibodies, MonoclonalAntigens, NeoplasmDrug Resistance, NeoplasmHumansNeoplasmsT-Lymphocytes, Helper-InducerAntibodies, MonoclonalAntigens, Neoplasm

Identifiers

PMID20028761
PMCPMC2802861
OpenAlexW2146602833

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.